Project ALS

Project ALS identifies and funds the most promising scientific research that will lead to the first effective treatments and, ultimately, a cure for ALS.

[Project ALS @ProjectALSorg]

To the Project ALS Family: We are proud to announce that prosetin, a novel ALS drug candidate developed at the Project ALS Therapeutics Core at Columbia, has been acquired for commercial development by a new company, ProJenX. Read the press release here: https://t.co/NSwpqCMnKX

[Project ALS @ProjectALSorg]

This past Sunday, July 26th, we celebrated the Americans with Disabilities Act (ADA) 36th Anniversary.

Project ALS is proud to support the Americans with Disabilities Act (ADA) 36th Anniversary. Learn how you can too, here: https://t.co/UgH0a9qX6o #ADA36 #ThanksToTheADA

[Project ALS @ProjectALSorg]

sorry we forgot our password.

we were also a bit busy continuing our mission of finding and funding a cure for #ALS.

anyway, we're back.

[Project ALS @ProjectALSorg]

Most importantly, the workshop laid the foundation for a new era of collaboration. Read the full workshop recap to see how Project ALS and the Packard Center are reshaping ALS research through partnership, innovation, and urgency.

https://t.co/7jyZN6TthM

[Project ALS @ProjectALSorg]

ALS affects motor neurons, the critical nerve cells in the brain and spinal cord that enable movement. But these cells can’t be biopsied to study in a lab. So how can we investigate what is happening to a motor neuron inside a person living with #ALS?

[Project ALS @ProjectALSorg]

For scientists working to understand how ALS begins and progresses, developing better lab-based models is essential. Over three days, participants shared new findings, pressing frustrations, and bold ideas to push science forward.

[Project ALS @ProjectALSorg]

To learn more about the NIH budget and grant-making process, visit https://t.co/FcVcp9Hpll or https://t.co/pHkFCtvMGF.

Project ALS remains committed to full transparency as this situation unfolds, and to our mission: finding a cure for ALS.

[Project ALS @ProjectALSorg]

...rely on for access to potential therapies.
We urge you to contact your local representatives—people living with ALS, and anyone affected by disease, deserve better.
The @alsassociation has created a resource to connect you with your Members of Congress: https://t.co/ta7OYP2fNI

[Project ALS @ProjectALSorg]

The NIH is the vital ecosystem within which the United States has become a global leader in healthcare and drug development. The proposed cuts threaten critical preclinical and clinical research, and would disrupt the entire drug development pipeline that people living with ALS..

[Project ALS @ProjectALSorg]

While Project ALS research currently remains on track, it will be extraordinarily difficult to keep pace with our progress if the planned cuts to NIH become reality.

[Project ALS @ProjectALSorg]

Thanks to NIH funding, Project ALS has been able to take a laser-focused approach to ALS research programs and the pursuit of ambitious blue-sky initiatives.

[Project ALS @ProjectALSorg]

Project ALS is concerned by proposed cuts to the National Institutes of Health (NIH).

Science is our most powerful tool in the fight against disease. NIH funding— over $47 billion annually— has been vital in advancing ALS research, including at the Project ALS Therapeutics Core.

[S. Preston @PootPoot]

Today ONLY if you purchase any item from the website, a portion of proceeds from your order will go directly to @ProjectALSorg ! This is the second time this year we’ve had the awesome opportunity to work with them and help raise some money!

[Project ALS @ProjectALSorg]

@RotoWear once again proving what's possible when we come together as a community. Thank you for all you do to fight ALS. ❤️

[RotoWear @RotoWear]

We’re proud to have donated $167,312.32 to @ProjectALSorg so far with proceeds from our Baseball Is The Best shirt! Thank you to everyone who purchased a shirt in support of @SlangsOnSports and helped in the mission to end ALS.

🔥👕 available only at:
https://t.co/yR0mrPyxtH

👇 donate directly:
https://t.co/ehnXcFJZPw

[Project ALS @ProjectALSorg]

@RotoWear @SlangsOnSports @PitchingNinja You are so incredible! We are so grateful to be fighting alongside you!

[Project ALS @ProjectALSorg]

Discover the critical work shaping the future of Project ALS research at our Town Hall. Join us as we discuss emerging disease models, motor neuron rejuvenation, and the development of potential therapies for ALS.

Sign up for the virtual town hall today: https://t.co/b4fZKkLoDu

[Project ALS @ProjectALSorg]

@matthewcerrone @RotoWear @PitchingNinja @SlangsOnSports Thank you for your support. ❤️

[Project ALS @ProjectALSorg]

Join us Nov. 14th at 11AM for The Alex and Jaci Hermstad Rare Disease Trailblazer Series. Hear from patients, families, advocates, and scientists working together toward a future free of ALS.

Register: https://t.co/toRtSsweZ4

[Project ALS @ProjectALSorg]

@NicoleWilsonNY @AaronLazar @rannellswotd @SaraBareilles Thank you for capturing this event! ❤️

[Project ALS @ProjectALSorg]

@muniba_mazari Thank you so much for being a part of this special night. ❤️